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Erratum to: Screening newborns for metabolic disorders based on targeted metabolomics using tandem mass spectrometry

Yoon HR

The original published article contains an inaccurate statement in Acknowledgements section.
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Turner syndrome with spinal hemorrhage due to vascular malformation

Yu MK, Jung MK, Kim KE, Kwon AR, Chae HW, Kim DH, Kim HS

Turner syndrome (TS) is a relatively common chromosomal disorder and is associated with a range of comorbidities involving the cardiovascular system. Vascular abnormalities, in particular, are a common finding in...
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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes

Jeong HA, Park YK, Jung YS, Nam MH, Nam HK, Lee KH, Rhie YJ

Hyponatremia and hyperkalemia in infancy can be attributed to various causes, originating from a variety of renal and genetic disorders. Pseudohypoaldosteronism type 1 (PHA1) is one of these disorders, causing...
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Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene

Jung JY, Yang S, Jeong EH, Lee HC, Lee YM, Han HS, Yi KH

Turner syndrome is the most common chromosomal disorder in girls. Various phenotypic features show depending upon karyotype from normal female through ambiguous genitalia to male. Usually, Turner girls containing 45,X/46,XY...
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Cerebral salt-wasting syndrome after hematopoietic stem cell transplantation in adolescents: 3 case reports

Jeon YJ, Lee HY, Jung IA, Cho WK, Cho B, Suh BK

Cerebral salt-wasting syndrome (CSWS) is a rare disease characterized by a extracellular volume depletion and hyponatremia induced by marked natriuresis. It is mainly reported in patients who experience a central...
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Blood glucose levels within 7 days after birth in preterm infants according to gestational age

Yoon JY, Chung HR, Choi CW, Yang SW, Kim BI, Shin CH

PURPOSE: This study investigated blood glucose levels in preterm babies according to gestational age (GA). METHODS: Subjects were 141 preterm infants with a GA
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Incidence trends and associated factors of diabetes mellitus in Korean children and adolescents: a retrospective cohort study in Busan and Gyeongnam

Lee JH, Kim YM, Kwak MJ, Kim SY, Kim HJ, Cheon CK, Chung WY, Choi IJ, Hong SY, Chueh HW, Yoo JH

PURPOSE: This study investigated the incidence trends and associated factors of type 1 (T1DM) and type 2 diabetes mellitus (T2DM) in children and adolescents under 15 years of age in...
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Risk factors of vitamin D deficiency in children with epilepsy taking anticonvulsants at initial and during follow-up

Lee SH, Yu J

PURPOSE: Vitamin D status was evaluated in children with epilepsy taking anticonvulsants to determine the prevalence and risk factors of vitamin D deficiency. METHODS: This study was designed as both a...
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Value of serum 1,5-anhydroglucitol measurements in childhood obesity in the continuum of diabetes

Yoo HY, Kwak BO, Son JS, Kim KS, Chung S

PURPOSE: The prevalence of type 2 diabetes mellitus (T2DM) and obesity are currently increasing. Accordingly, the concept of "preventing diabetes" in high-risk groups has become more important in diabetic care,...
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Guidelines for genetic skeletal dysplasias for pediatricians

Cho SY, Jin DK

Skeletal dysplasia (SD) is a kind of heterogeneous genetic disorder characterized by abnormal growth, development, differentiation, and maintenance of the bone and cartilage. The patients with SD most likely to...
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Endocrine and metabolic emergencies in children: hypocalcemia, hypoglycemia, adrenal insufficiency, and metabolic acidosis including diabetic ketoacidosis

Kim SY

It is important to fast diagnosis and management of the pediatric patients of the endocrine metabolic emergencies because the signs and symptoms of these disorders are nonspecific. Delayed diagnosis and...
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